A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475573



Internal ID21133126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94336189..94336817hg38UCSC Ensembl
chr12:94729965..94730593hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005399
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475573
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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